Willgerodt rearrangement

Named after  | Conrad Willgerodt
Reaction type  | Rearrangement reaction
Identifiers
RSC ontology ID  | RXNO:0000185

The Willgerodt rearrangement or Willgerodt reaction is an organic reaction converting an aryl alkyl ketone, alkyne, or alkene to the corresponding amide by reaction with ammonium polysulfide, named after Conrad Willgerodt.[1][2][3][4] The formation of the corresponding carboxylic acid is a side reaction resulting from hydrolysis of the amide. When the alkyl group is an aliphatic chain (n typically 0 to 5), multiple reactions take place with the amide group always ending up at the terminal end. The net effect is thus migration of the carbonyl group to the end of the chain and oxidation.

General scheme for the Willgerodt rearrangement

An example with modified reagents (sulfur, concentrated ammonium hydroxide and pyridine) is the conversion of acetophenone to 2-phenylacetamide and phenylacetic acid[5]

The Willgerodt rearrangement using acetophenone

## Willgerodt–Kindler reaction

Willgerodt–Kindler reaction

Named after  | Conrad Willgerodt
Karl Kindler
Reaction type  | Rearrangement reaction
Identifiers
Organic Chemistry Portal  | willgerodt-kindler-reaction
RSC ontology ID  | RXNO:0000186

The related Willgerodt–Kindler reaction[6] takes place with elemental sulfur and an amine like morpholine. The initial product is a thioamide for example that of acetophenone[7] which can again be hydrolyzed to the amide. The reaction is named after Karl Kindler (de)

The Kindler modification of the Willgerodt rearrangement

A possible reaction mechanism for the Kindler variation is depicted below:[8]

The likely reaction mechanism for the Kindler modification.

The first stage of the reaction is basic imine formation by the ketone group and the amine group of morpholine to give an enamine. This reacts as a nucleophile with electrophilic sulfur, similar to an Stork enamine alkylation reaction.[verification needed] The actual rearrangement reaction takes place when the amine group attacks the thiocarbonyl in a nucleophilic addition temporarily forming an aziridine and the thioacetamide by tautomerization.

## References

1. ↑ Willgerodt, Conrad (1887). "Ueber die Einwirkung von gelbem Schwefelammonium auf Ketone und Chinone". Berichte der Deutschen Chemischen Gesellschaft 20 (2): 2467–2470. doi:10.1002/cber.18870200278. https://zenodo.org/record/1425499.
2. ↑ Willgerodt, Conrad (1888). "Ueberführung von Ketonen und Aldehyden in Säuren und Säureamide mittelst gelben Schwefelammoniums". Berichte der Deutschen Chemischen Gesellschaft 21 (1): 534–536. doi:10.1002/cber.18870200278. https://zenodo.org/record/1425499.
3. ↑ Carmack, Marvin; F. DeTar, DeLos (1946). "The Willgerodt and Kindler Reactions. III. Amides from Acetylenes and Olefins; Studies Relating to the Reaction Mechanisms". Journal of the American Chemical Society 68 (10): 2029–2033. doi:10.1021/ja01214a048.
4. ↑ Carmack, Marvin; Spielman, M. A. (1946). "The Willgerodt Reaction". Organic Reactions 3: 83–107. doi:10.1002/0471264180.or003.02. ISBN 9780471005285.
5. ↑ The Willgerodt Reaction. II. A Study of Reaction Conditions with Acetophenone and Other KetonesDeLos F. DeTar and Marvin Carmack J. Am. Chem. Soc. 1946, 68(10), 2025 - 2029. (doi:10.1021/ja01214a047)
6. ↑ Karl Kindler (1923). "Studien über den Mechanismus chemischer Reaktionen. Erste Abhandlung. Reduktion von Amiden und Oxydation von Aminen". Liebigs Annalen 431 (1): 187–230. doi:10.1002/jlac.19234310111.
7. ↑ Organic Syntheses, Coll. Vol. 9, p.99 (1998); Vol. 74, p.257 (1997). (Article)
8. ↑ Name Reactions and Reagents in Organic Synthesis Bradford P. Mundy, Michael G. Ellerd, Frank G. Jr. Favaloro 2005 ISBN 0-471-22854-0

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